RISS 학술연구정보서비스

검색

인기 검색어

    다국어 입력

    http://chineseinput.net/에서 pinyin(병음)방식으로 중국어를 변환할 수 있습니다.

    변환된 중국어를 복사하여 사용하시면 됩니다.

    예시)
    • 中文 을 입력하시려면 zhongwen을 입력하시고 space를누르시면됩니다.
    • 北京 을 입력하시려면 beijing을 입력하시고 space를 누르시면 됩니다.
    닫기
    KCI등재 SCIE

    A branched TAT cell-penetrating peptide as a novel delivery carrier for the efficient gene transfection

    한글로보기

    https://www.riss.kr/link?id=A103818298

    • 0

      상세조회
    • 0

      다운로드
    서지정보 열기
    • 내보내기
    • 내책장담기
    • 공유하기
    • 오류접수

    부가정보

    다국어 초록 (Multilingual Abstract) kakao i 다국어 번역

    Background: Cell penetrating peptides (CPPs) as one class of non-viral vectors, have been widely explored as a delivery tool due to their cell-penetrating capability with low cytotoxicity. However, CPPs have reported to have low gene transfection efficiency mainly due to the fact that DNA is larger than other biomolecules. On the other hand, the conventional linear CPPs are unstable for constructing the DNA complexes with it. Thus, here we designed a branched CPP using disulfide bridges based on the linear TAT peptide, to enhance the gene delivery efficiency in a better way. Results: The branched TAT (BTAT) was synthesized by the DMSO oxidation method and showed high-molecularweight about 294 kDa. The resulting BTAT was complexed with plasmid green fluorescence protein (pGFP) gene at various N/P ratios. The gene transfection efficiency was assessed on HeLa cells after treating with BTAT/pGFP complexes, showed high gene transfection efficiency as conformed by flowcytometry followed by confocal laser scanning microscopy (CLSM) visualization. Conclusion: The novel BTAT/pGFP complex exhibited significantly higher stability and redox cleavability by reducing agent. In addition, BTAT showed higher transfection efficiency approximately 40-fold than those of the TAT and mTAT complexes. Our primary experiments demonstrated the potential of BTAT as a suitable candidate for gene delivery and it could be applied for various types of gene delivery platforms. Abbreviations: AAS, Antibiotic antimycotic solution; BTAT, Branched TAT; CPPs, Cell penetrating peptides; DMEM, Dulbecco’s Modified Eagle’s Medium; DMSO, Dimethyl sulfoxide; FACS, Fluorescence-activated cell sorting; FBS, Fetal bovine serum; GSH, Glutathione; HEPES, 2-[4-(2-hydroxyethyl) piperazin-1-yl] ethanesulfonic acid; mTAT, Modified TAT; PEI, Poly (ethyleneimine), CLSM, confocal laser scanning microscope; pGFP, Plasmid green fluorescence protein; TEM, Transmission electron microscopy
    번역하기

    Background: Cell penetrating peptides (CPPs) as one class of non-viral vectors, have been widely explored as a delivery tool due to their cell-penetrating capability with low cytotoxicity. However, CPPs have reported to have low gene transfection effi...

    Background: Cell penetrating peptides (CPPs) as one class of non-viral vectors, have been widely explored as a delivery tool due to their cell-penetrating capability with low cytotoxicity. However, CPPs have reported to have low gene transfection efficiency mainly due to the fact that DNA is larger than other biomolecules. On the other hand, the conventional linear CPPs are unstable for constructing the DNA complexes with it. Thus, here we designed a branched CPP using disulfide bridges based on the linear TAT peptide, to enhance the gene delivery efficiency in a better way. Results: The branched TAT (BTAT) was synthesized by the DMSO oxidation method and showed high-molecularweight about 294 kDa. The resulting BTAT was complexed with plasmid green fluorescence protein (pGFP) gene at various N/P ratios. The gene transfection efficiency was assessed on HeLa cells after treating with BTAT/pGFP complexes, showed high gene transfection efficiency as conformed by flowcytometry followed by confocal laser scanning microscopy (CLSM) visualization. Conclusion: The novel BTAT/pGFP complex exhibited significantly higher stability and redox cleavability by reducing agent. In addition, BTAT showed higher transfection efficiency approximately 40-fold than those of the TAT and mTAT complexes. Our primary experiments demonstrated the potential of BTAT as a suitable candidate for gene delivery and it could be applied for various types of gene delivery platforms. Abbreviations: AAS, Antibiotic antimycotic solution; BTAT, Branched TAT; CPPs, Cell penetrating peptides; DMEM, Dulbecco’s Modified Eagle’s Medium; DMSO, Dimethyl sulfoxide; FACS, Fluorescence-activated cell sorting; FBS, Fetal bovine serum; GSH, Glutathione; HEPES, 2-[4-(2-hydroxyethyl) piperazin-1-yl] ethanesulfonic acid; mTAT, Modified TAT; PEI, Poly (ethyleneimine), CLSM, confocal laser scanning microscope; pGFP, Plasmid green fluorescence protein; TEM, Transmission electron microscopy

    더보기

    참고문헌 (Reference)

    1 Kuai R, "Targeted delivery of cargoes into a murine solid tumor by a cell-penetrating peptide and cleavable poly(ethylene glycol)comodified liposomal delivery system via systemic administration" 8 : 2151-2161, 2011

    2 Guryanov I, "Starburst peptides containing HIV-1 TAT(48–60) : possibility of their use as carriers for DNA delivery into cell" 10 : 246-, 2004

    3 Modra K, "Polycation-mediated gene delivery : Challenges and considerations for the process of plasmid DNA transfection" 15 (15): 489-498, 2015

    4 Li JA, "Plasmid DNA could be delivered into Eimeria maxima unsporulated oocyst with gene gun system" 60 (60): 431-440, 2012

    5 Tzeng SY, "Non-viral gene delivery nanoparticles based on Poly(β-amino esters)for treatment of glioblastoma" 32 (32): 5402-5410, 2011

    6 Di Gioia S, "Nanocomplexes for gene therapy of respiratory diseases : Targeting and overcoming the mucus barrier" 34 : 8-24, 2015

    7 Koren E, "Multifunctional PEGylated 2C5-immunoliposomes containing pH-sensitive bonds and TAT peptide for enhanced tumor cell internalization and cytotoxicity" 160 (160): 264-273, 2012

    8 Kanning KC, "Motor neuron diversity in development and disease" 33 : 409-440, 2010

    9 Balbino TA, "Microfluidic assembly of pDNA/Cationic liposome lipoplexes with high pDNA loading for gene delivery" 32 (32): 1799-1807, 2016

    10 Sawant RR, "Liposomes as ‘smart’ pharmaceutical nanocarriers" 6 (6): 4026-, 2010

    1 Kuai R, "Targeted delivery of cargoes into a murine solid tumor by a cell-penetrating peptide and cleavable poly(ethylene glycol)comodified liposomal delivery system via systemic administration" 8 : 2151-2161, 2011

    2 Guryanov I, "Starburst peptides containing HIV-1 TAT(48–60) : possibility of their use as carriers for DNA delivery into cell" 10 : 246-, 2004

    3 Modra K, "Polycation-mediated gene delivery : Challenges and considerations for the process of plasmid DNA transfection" 15 (15): 489-498, 2015

    4 Li JA, "Plasmid DNA could be delivered into Eimeria maxima unsporulated oocyst with gene gun system" 60 (60): 431-440, 2012

    5 Tzeng SY, "Non-viral gene delivery nanoparticles based on Poly(β-amino esters)for treatment of glioblastoma" 32 (32): 5402-5410, 2011

    6 Di Gioia S, "Nanocomplexes for gene therapy of respiratory diseases : Targeting and overcoming the mucus barrier" 34 : 8-24, 2015

    7 Koren E, "Multifunctional PEGylated 2C5-immunoliposomes containing pH-sensitive bonds and TAT peptide for enhanced tumor cell internalization and cytotoxicity" 160 (160): 264-273, 2012

    8 Kanning KC, "Motor neuron diversity in development and disease" 33 : 409-440, 2010

    9 Balbino TA, "Microfluidic assembly of pDNA/Cationic liposome lipoplexes with high pDNA loading for gene delivery" 32 (32): 1799-1807, 2016

    10 Sawant RR, "Liposomes as ‘smart’ pharmaceutical nanocarriers" 6 (6): 4026-, 2010

    11 Thomas CE, "Kay Ma : Progress and problems with the use of viral vectors for gene therapy" 4 (4): 346-358, 2003

    12 Dixon JE, "Highly efficient delivery of functional cargoes by the synergistic effect of GAG binding motifs and cellpenetrating peptides" 113 (113): E291-E299, 2016

    13 Cohen-Avrahami M, "HIV-TAT enhances the transdermal delivery of NSAID drugs from liquid crystalline mesophases" 118 (118): 6277-6287, 2014

    14 Estrela JM, "Glutathione in cancer biology and therapy" 43 (43): 143-181, 2006

    15 Candolfi M, "Gene therapy-mediated delivery of targeted cytotoxins for glioma therapeutics" 107 (107): 20021-20026, 2010

    16 Kumar MD, "Gene therapy as a potential tool for treating neuroblastoma-a focused review" 23 (23): 115-124, 2016

    17 Jiang Q-Y, "Gene delivery to tumor cells by cationic polymeric nanovectors coupled to folic acid and the cell-penetrating peptide octaarginine" 32 (32): 7253-7262, 2011

    18 Lamichhane TN, "Exogenous DNA Loading into Extracellular Vesicles via Electroporation is Size-Dependent and Enables Limited Gene Delivery" 12 (12): 3650-3657, 2015

    19 Jun Yang, "Engineered biomaterials for development of nucleic acid vaccines" 한국생체재료학회 19 (19): 21-29, 2015

    20 Ghivizzani SC, "Direct retrovirus-mediated gene transfer to the synovium of the rabbit knee : Implications for arthritis gene therapy" 4 (4): 977-982, 1997

    21 Bonner DK, "Crosslinked linear polyethylenimine enhances delivery of DNA to the cytoplasm" 167 (167): 101-107, 2013

    22 Hansen MB, "Constrained and UV-activatable cell-penetrating peptides for intracellular delivery of liposomes" 164 (164): 87-94, 2012

    23 Raucher D, "Cell-penetrating peptides : strategies for anticancer treatment" 21 (21): 560-570, 2015

    24 Copolovici DM, "Cell-penetrating peptides : design, synthesis, and applications" 8 (8): 1972-1994, 2014

    25 Yue JH, "BMP2 gene delivery to bone mesenchymal stem cell by chitosan-g-PEI nonviral vector" 10 : 11-, 2015

    26 Jin E, "Acid-active cell-penetrating peptides for in vivo tumortargeted drug delivery" 135 (135): 933-940, 2013

    27 Paul A, "A nanobiohybrid complex of recombinant baculovirus and Tat/DNA nanoparticles for delivery of Ang-1 transgene in myocardial infarction therapy" 32 (32): 8304-8318, 2011

    더보기

    동일학술지(권/호) 다른 논문

    동일학술지 더보기

    더보기

    분석정보

    View

    상세정보조회

    0

    Usage

    원문다운로드

    0

    대출신청

    0

    복사신청

    0

    EDDS신청

    0

    동일 주제 내 활용도 TOP

    더보기

    주제

    연도별 연구동향

    연도별 활용동향

    연관논문

    연구자 네트워크맵

    공동연구자 (7)

    유사연구자 (20) 활용도상위20명

    인용정보 인용지수 설명보기

    학술지 이력

    학술지 이력
    연월일 이력구분 이력상세 등재구분
    2023 평가 해외DB학술지평가 신청대상 (해외등재 학술지 평가)
    2020-01-01 등재 등재학술지 유지 (해외등재 학술지 평가) KCI등재
    2017-01-01 등재 등재학술지 유지 (계속평가) KCI등재
    2013-01-01 등재 등재 1차 FAIL (등재유지) KCI등재
    2010-01-01 등재 등재학술지 유지 (등재유지) KCI등재
    2007-01-01 등재 등재학술지 선정 (등재후보2차) KCI등재
    2006-01-01 등재 등재후보 1차 PASS (등재후보1차) KCI등재후보
    2005-03-28 학회명변경 한글명 : 생체재료학회 -> 한국생체재료학회
    영문명 : 미등록 -> The Korean Society For Biomaterials
    KCI등재후보
    2005-03-28 학술지등록 한글명 : 생체재료학회지
    외국어명 : Biomaterials Research
    KCI등재후보
    2004-07-01 등재 등재후보학술지 선정 (신규평가) KCI등재후보
    더보기

    학술지 인용정보

    학술지 인용정보
    기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
    2016 0.32 0.32 0.3
    KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
    0.26 0.23 0.511 0.11
    더보기

    이 자료와 함께 이용한 RISS 자료

    나만을 위한 추천자료

    해외이동버튼